Marie-francoise Arthus
Montreal, QC, Canada
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
A Novel Form of Familial Vasopressin Deficient Diabetes Insipidus Transmitted in an X-linked Recessive Manner.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 27, 2021
Further evidence for functional recovery of AQP2 mutations associated with nephrogenic diabetes insipidus.
Journal: Physiological reports
Published: January 20, 2021
Erratum: Long-term outcome in inherited nephrogenic diabetes insipidus.
Journal: Clinical kidney journal
Published: January 04, 2021
Diurnal Variation of Urinary Fabry Disease Biomarkers during Enzyme Replacement Therapy Cycles.
Journal: International journal of molecular sciences
Published: July 24, 2020
Independent Registries Are Cost-Effective Tools to Provide Mandatory Postauthorization Surveillance for Orphan Medicinal Products.
Journal: Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research
Published: May 08, 2020
Long-term outcome in inherited nephrogenic diabetes insipidus.
Journal: Clinical kidney journal
Published: December 04, 2017
Analysis of globotriaosylceramide (Gb3) isoforms/analogs in unfractionated leukocytes, B lymphocytes and monocytes from Fabry patients using ultra-high performance liquid chromatography/tandem mass spectrometry.
Journal: Analytica chimica acta
Published: September 24, 2017
Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology.
Journal: Clinical kidney journal
Published: February 17, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026